3-(1-(tert-Butyldimethylsilyl)-1H-indol-5-yl)benzoic acid CAS 1228957-08-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1228957-08-1
Molecular FormulaC21H25NO2Si
Molecular Weight351.51 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(1-(tert-Butyldimethylsilyl)-1H-indol-5-yl)benzoic acid CAS 1228957-08-1 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-(1-(tert-Butyldimethylsilyl)-1H-indol-5-yl)benzoic acid.

3-(1-(tert-Butyldimethylsilyl)-1H-indol-5-yl)benzoic acid (CAS 1228957-08-1), molecular formula C21H25NO2Si and molecular weight 351.51 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C21H25NO2Si, 3-(1-(tert-Butyldimethylsilyl)-1H-indol-5-yl)benzoic acid contains a steroid core, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 351.51 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 3-(1-(tert-Butyldimethylsilyl)-1H-indol-5-yl)benzoic acid under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC21H25NO2Si
Molecular Weight351.51 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1

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